FDA.reportPublic FDA data

Salicylic Acid

Manufacturer
Chain Drug Consortium, LLC
Effective date
2025-10-08
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
monthly-update
Hydrated at
2026-06-03 17:38:11

Label at a glance#

ProductSalicylic Acid
Active ingredientSALICYLIC ACID
Label structure9 sections

Indications and uses

for the removal of corns and calluses relieves pain by removing corns and calluses

Dosage and administration

wash affected area and dry thoroughly apply one drop at a time with applicator, to sufficiently cover each corn/callus; let dry use cushions with hole centered over corn or callus to relieve pressure (additional cushions may be purchased separately) repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)

Label contents#

Full prescribing information#

​Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 17%w/w

Purpose

OTC - PURPOSE SECTION

Corn and callus remover

Uses

INDICATIONS & USAGE SECTION

  • for the removal of corns and calluses
  • relieves pain by removing corns and calluses

​Warnings

WARNINGS SECTION

Flammable

SAFE HANDLING WARNING SECTION

  • keep away from fire or flame
  • cap bottle tightly and store at room temperature away heat

Do not use

OTC - DO NOT USE SECTION

  • on irritated skin
  • on any area that is infected or reddened
  • if you are a diabetic, or if you have poor blood circulation, except under the advice and supervision of a doctor or podiatrist

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes
  • avoid inhaling vapors
  • if product gets into the eyes, flush with water for 15 minutes

Stop and ask a doctor if

OTC - STOP USE SECTION

discomfort persists, see your doctor or podiatrist

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

​Directions

DOSAGE & ADMINISTRATION SECTION

  • wash affected area and dry thoroughly
  • apply one drop at a time with applicator, to sufficiently cover each corn/callus; let dry
  • use cushions with hole centered over corn or callus to relieve pressure (additional cushions may be purchased separately)
  • repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)

Other information

OTHER SAFETY INFORMATION

store between 20°C to 30°C (68°F to 86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

camphor, castro oil, ethanol, ethyl ether, nitrocellulose

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

​Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Premier Value

Liquid Corn And Callus Remover

with Salicylic Acid

  • Cushions against Pain and Pressure
  • Removes corn and calluses safely

3 Cushions

1/3 FL OZ (9.8 mL)

Premier Value Liquid Corn and Callus Remover CardPremier Value Liquid Corn and Callus Remover Card

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130311917093925GTIN-13: 0311917093925
EAN-13: 0311917093925
GTIN-12: 311917093925
UPC-A: 311917093925
GTIN storage (14 digits): 00311917093925		Premier Value_Liquid Corn and Callus Card_41-030PV.jpg

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZ2
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ2
CAMPHOR (NATURAL)INACTIVE INGREDIENTN20HL7Q9412
CASTOR OILINACTIVE INGREDIENTD5340Y2I9G2
PYROXYLININACTIVE INGREDIENTKYR8BR2X6O2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68016-61068016-610-00, 68016-610-09

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (NATURAL)N20HL7Q941IACT
PYROXYLINKYR8BR2X6OIACT
CASTOR OILD5340Y2I9GIACT
SALICYLIC ACIDO414PZ4LPZACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
102024-12-11full-release2026-06-01 00:42:34

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 16 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CASTOR OILCASTOR OILD5340Y2I9GTABLET / ORAL17 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GINJECTION, SOLUTION / INTRAMUSCULAR525 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GSOLUTION / TOPICAL1.38 %w/wExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GTABLET, FILM COATED / ORAL15.29 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GSPRAY / NASALNAExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GTABLET, COATED / ORAL0.9 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GGEL / NASAL429 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GTABLET, DELAYED RELEASE / ORAL0.01 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GTABLET / SUBLINGUAL1.6 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GOINTMENT / TOPICAL14.9 %w/wExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GCAPSULE, EXTENDED RELEASE / ORAL47 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GINJECTION / INTRAMUSCULAR885 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GCAPSULE / ORAL1.04 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GGRANULE, FOR SUSPENSION / ORAL128 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GTABLET, EXTENDED RELEASE / ORAL23.27 mgExact identifier — unii candidate
16 equally ranked IID candidates
CASTOR OILCASTOR OILD5340Y2I9GEMULSION / OPHTHALMIC32 mgExact identifier — unii candidate
16 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
521ecd26-793d-0330-e063-6394a90a0d2bcbd07fb2-587c-4c0c-b4a9-3b49c22cc5622026-05-18WarningsExact identifier
spl set id: cbd07fb2-587c-4c0c-b4a9-3b49c22cc562

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.